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HRID 852444作成日:2026年10月25日

4-(4-Benzylpiperazin-1-yl)aniline → N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/852444

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-Benzylpiperazin-1-yl)anilineHCID 737259—
反応物4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chlorideHCID 11066000—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamideHCID 22499401104.6%

反応手順

A mixture of 4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carbonyl chloride (0.185 mole) in DCM (1500 ml) and triethylamine (50 ml) was stirred on an ice-bath for 5 minutes. 4-[4-(Phenylmethyl)-1-piperazinyl]-benzenamine (0.37 mole) in DCM (500 ml) was added dropwise. The mixture was stirred for 3 hours. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. The residue was triturated in DIPE. The precipitate was filtered off and dried, yielding 99.8 g of N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4′-(trifluoro-methyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 5, melting point 180° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07253157B2
出典データセットuspto-grants-2007_08
ORD IDord-c8a041bbd1d24bd4ad7926b86b2edd7b
出典メモuspto-grants-2007_08